Li Zhen-Ling, Gong Ming, Xu Shao-Hua, Huang Fan-Zhou, Chen Yan-Rong, Ma Yi-Gai
Department of Hematology, China-Japan Friendship Hospital, Beijing 100029, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2005 Oct;13(5):867-70.
To determine the efficacy and tolerance to cyclosporine A (CsA) based therapy in patients with myelodysplastic syndrome (MDS), 16 patients with MDS consisting of 10 refractory anemia (RA) and 6 refractory anemia with accessory blasts less than 10% (RAEB-1) were analyzed. Five patients had hypocellular bone marrows and 11 patients had normocellular or hypercellular marrows. The dose of CsA was 2.5-5.5 mg/(kg.d) for 2 weeks to 2 years (mean 8 months). Two out of 16 patients were treated with CsA alone, 14 patients were treated with CsA, recombinant human erythropoietin, androgens, 1, 25 dihydroxy vitamin D(3) or two or three of them combination with CsA. Treatment responses were classified according to the International Working Group (IWG) criteria as complete remission (CR), partial remission (PR), hematological improvement (HI) and no response (NR). Patients who obtained CR, PR or HI were defined as responders. The results showed that HI was observed in 12 patients, PR in 2 patients and NR in 2 patients. Total response rate was 87.5%. Response rates shown in neutrophil lineage, platelet and erythroid lineage were 83.3%, 66.7% and 60%, respectively; their shortest time required to obtain some hematologic improvement after initiation of CsA therapy was 2 weeks, 1 month and 1 month, respectively. Of 13 patients being transfusion-dependent before treatment, 3 patients did not need transfusion any more and 5 showed the reduced transfusion requirements after CsA therapy. In 10 patients with RA, 9 responded to CsA. Of 6 patients with RAEB, 1 patient had no response and died of RAEB-t and 5 patients had transient responses. One of the latter transformed to CMML and two relapsed. The total response rate decreased to 50% in the patients with CsA therapy lasting more than 3 months at the end of following-up. The adverse effects included hirsutism, hyperplastic gingiva, reversible hepatic and renal dysfunction. In conclusion, the usefulness of CsA based therapy for MDS-RA and RAEB-1 with any marrow cellularity is useful, the CsA dose of 3-5 mg/(kg.d) is safe and efficacious.
为确定环孢素A(CsA)治疗方案对骨髓增生异常综合征(MDS)患者的疗效及耐受性,分析了16例MDS患者,其中包括10例难治性贫血(RA)和6例原始细胞小于10%的难治性贫血伴原始细胞增多(RAEB-1)。5例患者骨髓细胞减少,11例患者骨髓细胞正常或增多。CsA剂量为2.5 - 5.5mg/(kg·d),疗程2周 - 2年(平均8个月)。16例患者中2例仅接受CsA治疗,14例患者接受CsA、重组人促红细胞生成素、雄激素、1,25 - 二羟维生素D(3)或其中两三种与CsA联合治疗。治疗反应根据国际工作组(IWG)标准分为完全缓解(CR)、部分缓解(PR)、血液学改善(HI)和无反应(NR)。获得CR、PR或HI的患者被定义为反应者。结果显示,12例患者出现HI,2例患者出现PR,2例患者出现NR。总反应率为87.5%。中性粒细胞系、血小板系和红系的反应率分别为83.3%、66.7%和60%;CsA治疗开始后获得某些血液学改善所需的最短时间分别为2周、1个月和1个月。治疗前13例依赖输血的患者中,3例不再需要输血,5例CsA治疗后输血需求减少。10例RA患者中,9例对CsA有反应。6例RAEB患者中,1例无反应,死于RAEB-t,5例有短暂反应。其中1例转化为慢性粒 - 单核细胞白血病(CMML),2例复发。随访结束时,CsA治疗持续超过3个月的患者总反应率降至50%。不良反应包括多毛症、牙龈增生、可逆性肝肾功能障碍。总之,基于CsA的治疗方案对任何骨髓细胞状态的MDS-RA和RAEB-1均有效,3 - 5mg/(kg·d)的CsA剂量安全有效。